Physicochemical insights of irradiation-enhanced hydroxyl radical generation from ZnO nanoparticles

The widespread use of zinc oxide nanoparticles (ZnO NPs) has raised environmental and human health concerns owing to their significant cytotoxicity. Although their cytotoxic effects have been associated with reactive oxygen species (ROS), the physicochemical mechanism underlying this phenomenon remains poorly understood. In this study, the physicochemical properties of ZnO NPs were systematically investigated in relation to their effect on ROS generation. Factors that were found to affect hydroxyl radical ((OH)-O-center dot) generation included: NP concentration, irradiation, NP hydrodynamic size, localized pH, ionic strength, NP zeta-potential, and dissolved oxygen levels. The mechanism by which (OH)-O-center dot was generated under alkaline conditions was found to obey first-order reaction kinetics that followed the conversion of OH-anions and dissolved O-2 to (OH)-O-center dot. Based on these findings, we propose that ZnO NP cytotoxicity involves (OH)-O-center dot adsorption to the nanoparticle surface, creating a highly localized source of ROS capable of potentiating oxidative damage to cellular structures. This hypothesis was evaluated with time-resolved intracellular calcium [Ca](i) imaging that irradiated ZnO NPs triggered cytoplasmic calcium influxes and facilitated nuclear degradation. Together these findings present a novel physicochemical mechanism for (OH)-O-center dot generation from ZnO NPs with significant implications for nanoparticle cytotoxicity and their relation to human health.